Kenna MA - Search Results

1

Neuroimaging in Kabuki syndrome and another KMT2D-related disorder.

Stadelmaier RT, Kenna MA, Barrett D, Mullen TE, Bodamer O, Agrawal PB, Robson CD, Wojcik MH. Stadelmaier RT, et al. Among authors: kenna ma. Am J Med Genet A. 2021 Dec;185(12):3770-3783. doi: 10.1002/ajmg.a.62450. Epub 2021 Aug 9. Am J Med Genet A. 2021. PMID: 34369642 Free PMC article.

2

Craniofacial, temporal bone, and audiologic abnormalities in the spectrum of hemifacial microsomia.

Rahbar R, Robson CD, Mulliken JB, Schwartz L, Dicanzio J, Kenna MA, McGill TJ, Healy GB. Rahbar R, et al. Among authors: kenna ma. Arch Otolaryngol Head Neck Surg. 2001 Mar;127(3):265-71. doi: 10.1001/archotol.127.3.265. Arch Otolaryngol Head Neck Surg. 2001. PMID: 11255470

3

The presentation and management of nasal dermoid: a 30-year experience.

Rahbar R, Shah P, Mulliken JB, Robson CD, Perez-Atayde AR, Proctor MR, Kenna MA, Scott MR, McGill TJ, Healy GB. Rahbar R, et al. Among authors: kenna ma. Arch Otolaryngol Head Neck Surg. 2003 Apr;129(4):464-71. doi: 10.1001/archotol.129.4.464. Arch Otolaryngol Head Neck Surg. 2003. PMID: 12707196

4

Additional clinical manifestations in children with sensorineural hearing loss and biallelic GJB2 mutations: who should be offered GJB2 testing?

Kenna MA, Rehm HL, Robson CD, Frangulov A, McCallum J, Yaeger D, Krantz ID. Kenna MA, et al. Am J Med Genet A. 2007 Jul 15;143A(14):1560-6. doi: 10.1002/ajmg.a.31706. Am J Med Genet A. 2007. PMID: 17455295

5

Temporal bone abnormalities in children with GJB2 mutations.

Kenna MA, Rehm HL, Frangulov A, Feldman HA, Robson CD. Kenna MA, et al. Laryngoscope. 2011 Mar;121(3):630-5. doi: 10.1002/lary.21414. Epub 2011 Feb 4. Laryngoscope. 2011. PMID: 21298644 Free PMC article.

6

Enlarged Vestibular Aqueduct and Cochlear Implants: The Effect of Early Counseling on the Length of Time Between Candidacy and Implantation.

Bostic K, Lewis RM, Chai B, Manganella JL, Barrett DL, Kawai K, Kenna MA, Stiles DJ, Clark T. Bostic K, et al. Among authors: kenna ma. Otol Neurotol. 2018 Feb;39(2):e90-e95. doi: 10.1097/MAO.0000000000001663. Otol Neurotol. 2018. PMID: 29315182

7

Otolaryngologic Manifestations of Klippel-Feil Syndrome in Children.

Kenna MA, Irace AL, Strychowsky JE, Kawai K, Barrett D, Manganella J, Cunningham MJ. Kenna MA, et al. JAMA Otolaryngol Head Neck Surg. 2018 Mar 1;144(3):238-243. doi: 10.1001/jamaoto.2017.2917. JAMA Otolaryngol Head Neck Surg. 2018. PMID: 29372238 Free PMC article.

8

Ambulatory Visits for Otitis Media before and after the Introduction of Pneumococcal Conjugate Vaccination.

Kawai K, Adil EA, Barrett D, Manganella J, Kenna MA. Kawai K, et al. Among authors: kenna ma. J Pediatr. 2018 Oct;201:122-127.e1. doi: 10.1016/j.jpeds.2018.05.047. Epub 2018 Jun 27. J Pediatr. 2018. PMID: 29958675

9

Validation of a portable hearing assessment tool: Agilis Health Mobile Audiogram.

Manganella JL, Stiles DJ, Kawai K, Barrett DL, O'Brien LB, Kenna MA. Manganella JL, et al. Among authors: kenna ma. Int J Pediatr Otorhinolaryngol. 2018 Oct;113:94-98. doi: 10.1016/j.ijporl.2018.04.010. Epub 2018 Apr 16. Int J Pediatr Otorhinolaryngol. 2018. PMID: 30174018

10

A novel missense mutation in TFAP2B associated with Char syndrome and central diabetes insipidus.

Edward HL, D'Gama AM, Wojcik MH, Brownstein CA, Kenna MA, Grant PE, Majzoub JA, Agrawal PB. Edward HL, et al. Among authors: kenna ma. Am J Med Genet A. 2019 Jul;179(7):1299-1303. doi: 10.1002/ajmg.a.61150. Epub 2019 Apr 22. Am J Med Genet A. 2019. PMID: 31012281

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